Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 2-Cyclohexyloxirane | HCID 94264 | 62% |
Reaktionsschritte
Sodium hydride (4.5 g, 187.5 mmol) and trimethylsulfoxonium iodide (41.25 g, 187.5 mmol) were combined in a 3-neck flask equipped with a mechanical stirrer and an addition funnel. Dimethyl sulfoxide (DMSO) was added slowly over a 30 min period, until 200 mL had been added. Gas was evolved throuqhout the addition. A solution of cyclohexane carboxaldehyde (21.8 mL, 180 mmol) in 50 mL of DMSO was added dropwise to the reaction mixture over a 15 min period. The reaction mixture was heated to 55° C. and stirred at 55° C. for 30 min. The reaction mixture was cooled to ambient temperature and poured into 500 mL of water. The aqueous solution was extracted with 3×100 mL of diethyl ether. The combined ether extracts were washed with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The crude product was distilled (44° C., 0.1 mm) to give 14 g (62% yield) of 1-cyclohexyl ethylene oxide as a clear colorless liquid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04963568 |
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| Quelldatensatz | uspto-grants-1990_10 |
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| ORD ID | ord-cfad13b0da77481193ca16c0bb4d08d3 |
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| Quellennotiz | uspto-grants-1990_10 |
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